Cancer therapy based on tumor associated antigens derived from cyclin d1
a technology of cyclin d1 and tumors, applied in the field of cyclin-derived peptides, can solve the problem of not providing precise information as to the use of the antigens transcribed from these genes
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1. Identification and Characterization of Peptides as Used According to the Present Invention
[0093]In general, the peptides as used according to the present invention were identified using the XPRESIDENT® technology as described (see, for example, Weinschenk et al. Integrated Functional Genomics Approach for the Design of Patient-individual Antitumor Vaccines, CANCER RESEARCH 62, 5818-5827, Oct. 15, 2002) on the basis of renal cancer cells. The average overexpression of cyclin D1 (CCND1) in ccRCC against the average expression in normal tissues was 3.0-fold, and 5.7-fold in primary tumors and 5.4-fold in metastases. 55% of primary tumors showed an overexpression against normal kidney.
2. HLA-Restriction of the Peptides as Identified
[0094]For CCN-001 and CCN-002, a good binding to HLA A*02 was predicted using the SYFPEITHI routine (Rammensee et al., 1997; Rammensee et al., 1999). Good binding of CCN-001 to HLA A*0201 was confirmed by an ELISA-based method (Sylvester-Hvid et al., 2002)...
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